Maximum Strength Mucinex Fast-max Day Time Cold And Flu And Night Time Cold And Flu
NDC Package 63824-511-40
Package Information
Maximum Strength Mucinex Fast-max Day Time Cold And Flu And Night Time Cold And Flu is do not take more than directed (see Overdose warning)do not take more than 12 caplets in any 24-hour periodadults and children 12 years of age and over: take 2 caplets every 4 hourschildren under 12 years of age: do not use. Marketed by Rb Health (us) Llc, this product is identified by NDC 63824-511 and is authorized under FDA application part341.
Identification & Billing
- RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
- RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
- RxCUI: 1110988 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
- RxCUI: 1233575 - acetaminophen 325 MG / diphenhydrAMINE HCl 12.5 MG / phenylephrine HCl 5 MG Oral Tablet
- RxCUI: 1233575 - acetaminophen 325 MG / diphenhydramine hydrochloride 12.5 MG / phenylephrine hydrochloride 5 MG Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 63824 - Rb Health (us) Llc
- 63824-511 - Maximum Strength Mucinex Fast-max Day Time Cold And Flu And Night Time Cold And Flu
- 63824-511-40 - 4 KIT in 1 CARTON / 1 KIT in 1 KIT * 6 TABLET in 1 BLISTER PACK * 4 TABLET in 1 BLISTER PACK
- 63824-511 - Maximum Strength Mucinex Fast-max Day Time Cold And Flu And Night Time Cold And Flu
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (63824-511). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 63824-511-40 identifies a specific commercial package of 4 kit in 1 carton / 1 kit in 1 kit * 6 tablet in 1 blister pack * 4 tablet in 1 blister pack of Maximum Strength Mucinex Fast-max Day Time Cold And Flu And Night Time Cold And Flu, labeled by Rb Health (us) Llc. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Rb Health (us) Llc on June 01, 2020. The current certification is valid through December 31, 2021.
How is this Rb Health (us) Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 63824051140. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.
